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Page 1
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations.
Hampe J, Cuthbert A, Croucher PJ, Mirza MM, Mascheretti S, Fisher S, Frenzel H, King K, Hasselmeyer A, MacPherson AJ, Bridger S, van Deventer S, Forbes A, Nikolaus S, Lennard-Jones JE, Foelsch UR, Krawczak M, Lewis C, Schreiber S, Mathew CG. Hampe J, et al. Lancet. 2001 Jun 16;357(9272):1925-8. doi: 10.1016/S0140-6736(00)05063-7. Lancet. 2001. PMID: 11425413
A common Fanconi anemia mutation in black populations of sub-Saharan Africa.
Morgan NV, Essop F, Demuth I, de Ravel T, Jansen S, Tischkowitz M, Lewis CM, Wainwright L, Poole J, Joenje H, Digweed M, Krause A, Mathew CG. Morgan NV, et al. Among authors: lewis cm. Blood. 2005 May 1;105(9):3542-4. doi: 10.1182/blood-2004-10-3968. Epub 2005 Jan 18. Blood. 2005. PMID: 15657175 Free article.
Association of DLG5 R30Q variant with inflammatory bowel disease.
Daly MJ, Pearce AV, Farwell L, Fisher SA, Latiano A, Prescott NJ, Forbes A, Mansfield J, Sanderson J, Langelier D, Cohen A, Bitton A, Wild G, Lewis CM, Annese V, Mathew CG, Rioux JD. Daly MJ, et al. Among authors: lewis cm. Eur J Hum Genet. 2005 Jul;13(7):835-9. doi: 10.1038/sj.ejhg.5201403. Eur J Hum Genet. 2005. PMID: 15841097
806 results